Variant #0000977209 (NC_000006.11:g.34392993C>T, NM_001203245.2:c.6G>A (RPS10))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.34392993C>T
DNA change (hg38) -
Published as RPS10(NM_001014.5):c.6G>A (p.(Leu2=))
ISCN -
DB-ID NUDT3_000002
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00083 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPS10-NUDT3 NM_001202470.2 -?/. - c.6G>A r.(?) p.(=)
RPS10 NM_001203245.2 -?/. - c.6G>A r.(?) p.(=)
NUDT3 NM_006703.3 -?/. - c.-32854G>A r.(?) p.(=)


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